3'-Chloroacetophenone

3'-Chloroacetophenone
  • CAS No.:99-02-5
Other grades of this product :
3'-Chloroacetophenone Basic information
Uses
Product Name:3'-Chloroacetophenone
Synonyms:M-CHLOROACETOPHENONE;1-(3-CHLOROPHENYL)ETHANONE;1-(3-chlorophenyl)-ethanon;3'-Chloroacetylphenone;Ethanone, 1-(3-chlorophenyl)-;3'-Chloroacetophenone 1-(3-Chlorophenyl)ethanone 3-Chloroacetophenone;3-Chloroacetophenone, 98+%;3'-CHLOROACETOPHENONE
CAS:99-02-5
MF:C8H7ClO
MW:154.59
EINECS:202-721-8
Product Categories:Aromatic Acetophenones & Derivatives (substituted);Adehydes, Acetals & Ketones;Chlorine Compounds;C7 to C8;Carbonyl Compounds;Ketones
Mol File:99-02-5.mol
3'-Chloroacetophenone Chemical Properties
Boiling point 227-229 °C(lit.)
density 1.191 g/mL at 25 °C(lit.)
refractive index n20/D 1.550(lit.)
Fp 221 °F
storage temp. Sealed in dry,Room Temperature
form Liquid
Specific Gravity1.191
color Clear colorless to yellow
Sensitive Lachrymatory
BRN 636318
InChIKeyUUWJBXKHMMQDED-UHFFFAOYSA-N
CAS DataBase Reference99-02-5(CAS DataBase Reference)
NIST Chemistry ReferenceAcetophenone, 3'-chloro-(99-02-5)
EPA Substance Registry SystemEthanone, 1-(3-chlorophenyl)- (99-02-5)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-36-20/21/22
Safety Statements 26-36-37/39-36/37/39-13-7/9
RIDADR UN 3416 6.1/PG 2
WGK Germany 3
19
Hazard Note Harmful/Irritant/Lachrymatory
TSCA Yes
HazardClass 6.1
PackingGroup II
HS Code 29147090
MSDS Information
ProviderLanguage
3'-Chloroacetophenone English
SigmaAldrich English
ACROS English
ALFA English
3'-Chloroacetophenone Usage And Synthesis
Uses3'-Chloroacetophenone can be used as a raw material for pharmaceutical synthesis, mainly for the synthesis of carbamazepine, a drug for the treatment of epilepsy, and as an intermediate for fine chemicals, pesticides, etc.
Chemical Propertiesclear colourless to yellow liquid
Synthesis Reference(s)The Journal of Organic Chemistry, 60, p. 2361, 1995 DOI: 10.1021/jo00113a013
General DescriptionThe activity of strain, Saccharomyces cerevisiae B5, on the reduction of 3′-chloroacetophenone was studied.

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